Search research articles
Contact Us
Filters
Showing results (231-240 of 332) with videos related to
Page
of 34
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
Marion Delcourt, Florence Riant, Josette Mancini, et al.
Annals of Neurology
|
May 31, 2017
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome
Domitille Gras, Christelle Cousin, Caroline Kappeler, et al.
NPJ Parkinson'S Disease
|
September 26, 2025
Sleep stage mixing is associated with poor prognosis in early Parkinson's disease
Pauline Dodet, Emmanuel During, Isabelle Arnulf, et al.
Cell Reports
|
January 20, 2021
Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements
Oriane Pourchet, Marie-Pierre Morel, Quentin Welniarz, et al.
Movement Disorders Clinical Practice
|
August 28, 2023
Night-Time Apomorphine Infusion: Who Are the Best Candidates?
Valérie Cochen De Cock, Pauline Dodet, Smaranda Leu-Semenescu, et al.
Scientific Reports
|
March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline
Quentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
Neurology
|
October 21, 2018
Predictors of alcohol responsiveness in dystonia
Johanna Junker, Valerie Brandt, Brian D Berman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients
Cyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Iscience
|
February 9, 2026
Modulation of striatal cAMP levels: A key pathway in the treatment of hyperkinetic movement disorders
Ruiyi Yuan, Emmanuel Roze, Mohamed Doulazmi, et al.
Journal of Medical Genetics
|
June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51
Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Page
of 34
Search research articles
Search
Showing results (231-240 of 332) with videos related to
Sort By:
Page
of 34
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
Marion Delcourt, Florence Riant, Josette Mancini, et al.
Annals of Neurology
|
May 31, 2017
A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome
Domitille Gras, Christelle Cousin, Caroline Kappeler, et al.
NPJ Parkinson'S Disease
|
September 26, 2025
Sleep stage mixing is associated with poor prognosis in early Parkinson's disease
Pauline Dodet, Emmanuel During, Isabelle Arnulf, et al.
Cell Reports
|
January 20, 2021
Loss of floor plate Netrin-1 impairs midline crossing of corticospinal axons and leads to mirror movements
Oriane Pourchet, Marie-Pierre Morel, Quentin Welniarz, et al.
Movement Disorders Clinical Practice
|
August 28, 2023
Night-Time Apomorphine Infusion: Who Are the Best Candidates?
Valérie Cochen De Cock, Pauline Dodet, Smaranda Leu-Semenescu, et al.
Scientific Reports
|
March 26, 2017
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline
Quentin Welniarz, Marie-Pierre Morel, Oriane Pourchet, et al.
Neurology
|
October 21, 2018
Predictors of alcohol responsiveness in dystonia
Johanna Junker, Valerie Brandt, Brian D Berman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients
Cyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Iscience
|
February 9, 2026
Modulation of striatal cAMP levels: A key pathway in the treatment of hyperkinetic movement disorders
Ruiyi Yuan, Emmanuel Roze, Mohamed Doulazmi, et al.
Journal of Medical Genetics
|
June 12, 2023
Congenital mirror movements are associated with defective polymerisation of RAD51
Oriane Trouillard, Pauline Dupaigne, Margaux Dunoyer, et al.
Page
of 34